Your search for "ehhadh" returned 274 TaqMan® SNP Genotyping Assays
enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase
The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]
1, 1300002P22RIK, ECHD, EHHADH, FRTS3, HD, L-PBE, LBFP, LBP, MEF, MFE, MFE1, MFP, MFP1, PBE, PBFE, PERMFE-1
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